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切向流深度过滤生产基于水疱性口炎病毒的重组载体。

Production of recombinant vesicular stomatitis virus-based vectors by tangential flow depth filtration.

机构信息

Bioprocess Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Sandtorstr. 1, 39106, Magdeburg, Germany.

Department of Chemical Engineering, Polytechnique Montréal, Montréal, Québec, Canada.

出版信息

Appl Microbiol Biotechnol. 2024 Feb 27;108(1):240. doi: 10.1007/s00253-024-13078-6.

Abstract

Cell culture-based production of vector-based vaccines and virotherapeutics is of increasing interest. The vectors used not only retain their ability to infect cells but also induce robust immune responses. Using two recombinant vesicular stomatitis virus (rVSV)-based constructs, we performed a proof-of-concept study regarding an integrated closed single-use perfusion system that allows continuous virus harvesting and clarification. Using suspension BHK-21 cells and a fusogenic oncolytic hybrid of vesicular stomatitis virus and Newcastle disease virus (rVSV-NDV), a modified alternating tangential flow device (mATF) or tangential flow depth filtration (TFDF) systems were used for cell retention. As the hollow fibers of the former are characterized by a large internal lumen (0.75 mm; pore size 0.65 μm), membrane blocking by the multi-nucleated syncytia formed during infection could be prevented. However, virus particles were completely retained. In contrast, the TFDF filter unit (lumen 3.15 mm, pore size 2-5 μm) allowed not only to achieve high viable cell concentrations (VCC, 16.4-20.6×10 cells/mL) but also continuous vector harvesting and clarification. Compared to an optimized batch process, 11-fold higher infectious virus titers were obtained in the clarified permeate (maximum 7.5×10 TCID/mL). Using HEK293-SF cells and a rVSV vector expressing a green fluorescent protein, perfusion cultivations resulted in a maximum VCC of 11.3×10 cells/mL and infectious virus titers up to 7.1×10 TCID/mL in the permeate. Not only continuous harvesting but also clarification was possible. Although the cell-specific virus yield decreased relative to a batch process established as a control, an increased space-time yield was obtained. KEY POINTS: • Viral vector production using a TFDF perfusion system resulted in a 460% increase in space-time yield • Use of a TFDF system allowed continuous virus harvesting and clarification • TFDF perfusion system has great potential towards the establishment of an intensified vector production.

摘要

基于细胞培养的载体疫苗和病毒疗法的生产越来越受到关注。所使用的载体不仅保留了感染细胞的能力,而且还能诱导强烈的免疫反应。我们使用两种重组水疱性口炎病毒(rVSV)载体构建体,进行了一项关于集成封闭的一次性灌注系统的概念验证研究,该系统允许连续收获和澄清病毒。使用悬浮 BHK-21 细胞和水疱性口炎病毒和新城疫病毒(rVSV-NDV)的融合溶瘤杂交物,我们使用改良的交替切向流设备(mATF)或切向流深度过滤(TFDF)系统进行细胞保留。由于前者的中空纤维具有较大的内部腔(0.75 毫米;孔径 0.65 微米),因此可以防止感染过程中形成的多核合胞体堵塞膜。然而,病毒颗粒完全被截留。相比之下,TFDF 过滤单元(腔 3.15 毫米,孔径 2-5 微米)不仅可以实现高活细胞浓度(VCC,16.4-20.6×106 细胞/mL),还可以连续收获和澄清载体。与优化的分批工艺相比,澄清透过液中获得了 11 倍更高的感染性病毒滴度(最高 7.5×106TCID/mL)。使用 HEK293-SF 细胞和表达绿色荧光蛋白的 rVSV 载体进行灌注培养,在透过液中获得了最高 VCC 为 11.3×106 细胞/mL 和感染性病毒滴度高达 7.1×106TCID/mL。不仅可以连续收获,还可以澄清。尽管相对于作为对照建立的分批工艺,细胞特异性病毒产率降低,但获得了增加的时空产率。关键点:• 使用 TFDF 灌注系统生产病毒载体导致时空产率增加了 460%• 使用 TFDF 系统允许连续收获和澄清病毒• TFDF 灌注系统在建立强化载体生产方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95c2/10899354/27e61ed540e6/253_2024_13078_Fig1_HTML.jpg

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